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rs587783130

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783130(A;A)
Make rs587783130(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18510828
GeneCDKL5
is asnp
is mentioned by
dbSNPrs587783130
ebirs587783130
HLIrs587783130
Exacrs587783130
Varsomers587783130
Maprs587783130
PheGenIrs587783130
hapmaprs587783130
1000 genomesrs587783130
hgdprs587783130
ensemblrs587783130
gopubmedrs587783130
geneviewrs587783130
scholarrs587783130
googlers587783130
pharmgkbrs587783130
gwascentralrs587783130
openSNPrs587783130
23andMers587783130
23andMe allrs587783130
SNP Nexus

SNPshotrs587783130
SNPdbers587783130
MSV3drs587783130
GWAS Ctlgrs587783130
Max Magnitude0
ClinVar
Risk rs587783130(A;A)
Alt rs587783130(A;A)
Reference rs587783130(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CDKL5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.18528948G>A
CLNSRC
CLNACC RCV000144802.1,